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PLATT CH19 BODY
MR UTT'S BODY STRUCTURE
Question | Answer |
---|---|
TYPES OF MUSCLE TISSUE? | SMOOTH, CARDIAC, SKELETAL |
BLOOD IS WHAT KIND OF TISSUE? | CONNECTIVE TISSUE |
SMOOTH MUSCLES ARE FOUND WHERE? | INTERNAL ORGANS |
CARDIAC MUSCLES ARE FOUND WHERE? | THE HEART ONLY |
SKELETAL MUSCLES ARE FOUND WHERE? | SKELETON, AND ASSIST WITH VOLUNTARY MOVEMENT |
ENDOPLASMIC RETICULUM | NETWORK OF TUBULES THROUGH THE NUCLEUS AND CYTOPLASM. |
GOLGI APPARATUS | A SERIES OF FLAT, MEMBRANOUS SACS. IT SECRETES SUBSTANCES SUCH AS MUCUS |
CENTRIOLES | ARE TO ORGANIZE THE SPINDLE FIBERS DURING CELL DIVISION. CENTRIOLES ARE NECESSARY FOR MITOSIS |
PHASES OF MITOSIS | PROPHASE, METAPHASE, ANAPHASE, TELOPHASE |
PROHASE | THE NUCLEUS MEMBRANE DISAPEARS. |
METAPHASE | SPINDLE FIBERS ALIGN THE CHROMOSOMES ALONG THE MIDDLE OF THE CELL NUCLEUS. |
ANAPHASE | OCCURES WHEN THE PAIRED CHROMOSOMES SEPARATE AT THE KENETOCHORES AND MOVE TO OPPOSITE SIDES OF THE CELL. |
TELOPHASE | CHROMOSOMES ARRIVE AT OPPOSITE POLES OF THE CELL, A NEW MEMBRANE FORMS AROUND THE NUCLEI. |
SUPERIOR OR CRANIAL | TOWARD THE HEAD END OF THE BODY; UPPER |
INFERIOR OR CAUDAL | AWAY FROM THE HEAD; LOWER |
ANTERIOR OR VENTRAL | FRONT |
POSTERIOR OR DORSAL | BACK |
MEDIAL | TOWARDS THE MIDLINE OF THE BODY |
LATERAL | AWAY FROM THE MIDLINE OF THE BODY |
PROXIMAL | TOWARD OR NEAREST THE TRUNK OR THE POINT OF ORIGIN |
DISTAL | AWAY FROM OR FARTHEST FROM THE TRUNK OR POINT OF ORIGIN. |
CORONAL PLANE | (FRONTAL PLANE) A VERTICAL PLANE RUNNING FROM SIDE TO SIDE. |
SAGITTAL PLANE | (MEDIAN PLANE) A VERTICAL PLANE RUNNING FROM FRONT TO BACK. |
AXIAL PLANE | (TRANSVERSE PLANE) A HORIZONTAL PLANE; DIVIDES THE BODY OR ANY PARTS INTO UPPER AND LOWER PARTS. |
MAIN CAVITIES | VENTRAL AND DORSAL CAVITIES |
SUB CAVITIES | THORACIC AND ABDOMINOPELVIC |
THORACIC CAVITY CONTAINS | HEART, LUNGS, TRACHEA, ESOPHAGUS, LARGE BLOOD VESSELS AND NERVES. |
ABDOMINOPELVIC CAVITY CONTAINS | GASTROINTESTINAL TRACT, KIDNEYS ADRENAL GLANDS, UROGENITAL SYSTEM, RECTUM |
DORAL CAVITY | UPPER PORTION, CRANIAL(BRAIN). LOWER PORTION (SPINAL CORD) |
ABDOMINAL REGIONS | RIGHT AND LEFT HYPOCHONDRIACE, RIGHT AND LEFT LUMBAR, RIGHT AND LEFT ILIAC, EPIGASTRIC, UMBILICAL, HYPOGASTRIC. |
ABDOMINAL QUADRANTS | RUQ, LUQ, RLQ, LLQ |
PERICARDIAL CAVITY | CONTAINS THE HEART |
ANTECUBITAL | BEND OF THE ELBOW |
AXILLARY | ARMPIT |
BUCCAL | CHEEK |
CERVICAL | NECK |
DELTOID | SHOULDER |
FEMORAL | THIGH |
GULTEAL | BUTTOCKS |
HEPATIC | LIVER |
LUMBAR | LOWER BACK |
OCCIPITAL | BACK OF HEAD |
PATELLAR | KNEECAP |
POPLITEAL | BEHIND THE KNEE |
PULMONARY | LUNGS |
RENAL | KIDNEY |
SURAL | CALF OF THE LEG |
THORACIC | CHEST |
VOLAR(PALMER) | PALM OF HAND |
DIFFUSION | THE MOVEMENT OF DISSOLVED PARTICLES FROM AN AREA OF GREATER CONCENTRATION TO AN AREA LESSER CONCENTRATION. |
OSMOSIS | A TYPE OF DIFFUSION IN WHICH WATER IS PULLED THROUGH A SEMIPERMEABLE MEMBRANE. |
FILTRATION | DISSOVED PARTICLES ARE DIFFUSED THROUGH MEMBRANES BUY ONLY MECHANICAL PRESSURE IS REQUIRED. |
PHAGOCYTOSIS | THE CELL ENGULFS A SOLID PARTICLE |
PINOCYTOSIS | THE CELL DRINKS THE FLUID REQUIRED. |
HEREDITY | THE GENETIC TRANSMISSION FROM PARENT TO CHILD |
ALBINISM | DISORDER; A RECESSIVE GENE MUTAITION THAT CAUSES LACK OF PIGMENT IN THE SKIN, HAIR, AND EYES. |
ATTENTION DIFICIT HYPERACTIVITY DISORDER(ADHD) | DISEASE: A PERSON WHO HAS DIFFICULTY ORGANIZING AND COMPLETING A TASK. |
CLEFT PALLET | DISORDER: DEFECT IN THE ROOF OF THE MOUTH THAT OCCURES WHEN THE PALATINE BONE DOES NOT CLOSE PROPERLY. |
COLOR DIFICIENCY | DISORDER; COLOR BLINDNESS |
CYSTIC FIBROSIS | DISEASE; MUCUS THAT BECOMES THICK, DRY AND STICKY. CLOGGING PASSAGES IN MANY OF THE BODYS ORGANS. |
DOWNS SYNDROME | DISORDER; CAUSE BY A PERSON WITH AND EXTRA CHROMOSOME. |
FRAGILE X SYNDROME | DISORDER; KNOWN AS MARTIN-BELL OR MARKER X SYNDROME. IS THE MOST COMMON FORM OF MENTAL RETARDATION. |
HEMOCHROMATOSIS | DISORDER; EFFECTS THE BODYS ACCUMULATION OF IRON. |
HEMOPHILIA | DISORDER; IN WHICH THE BLOOD COAGULATION TIME IS GREATLY INCREASED. |
KLINEFELTER'S SYNDROME | DISORDER; TESTICULAR FAILURE OCCURES THAT IS NOT EVIDENT UNTIL PUBERTY. TESTES ARE SMALL AND FIRM. ABNORMALLY LONG LEGS. |
MUSCULAR DYSTROPHY | DISEASE; GRADUAL ATROPHY AND WEAKENING OF THE MUSCLE. |
PHENYLKETONURIA (PKU) | DISORDER; RECESSIVE GEN MUTATION. UNABLE TO OXIDIZE AN AMINO ACID. MENTAL RETARDATION OCCURS DUE TO BRAIN DAMAGE. |
SICKLE CELL ANEMIA | DISORDER; RED BLOOD CELLS ARE SICKLE SHAPE, LIMITS OXIGEN TRANSPORTATION AND CAN CLOG SMALL CAPILLARIES. |
SPINA BIFIDA | DISORDER; POSTERIOR VERTEBRAL ARCH HAS A DEVELOPMENTAL ABNORMALY. |
TALIPES (CLUBFOOT) | DISORDER; DEFORMITY OF THE FOOT |
TAY-SACHS DISEASE (TSD) | DISORDER; A BABY WILL STOP MOVING AND SMILING AND BECOME PARALYZED, AND EVENTUALLY DIE. |
TURNER'S SYNDROME | DISORDER; FAILURE OF THE OVARIES TO RESPOND TO THE STIMULATION OF THE PITUITARY GLANDS. USUALLY HAVE A SHORT STATURE. |