Pitutary dwarfism
Made easy, Simple , simplified .
- Congenital: agenesis, aplasia, dysplasia. Traumatic.
- Infection: T.B., sarcoidosis.
- Neoplastic: cranio-pharyngioma, pituitary adenoma. Iatrogenic: surgical excision, irradiation.
- Congenital: agenesis, aplasia, dysplasia. Traumatic.
- Infection: T.B., sarcoidosis.
- Neoplastic: cranio-pharyngioma, pituitary adenoma. Iatrogenic: surgical excision, irradiation.
- normal size & wt.
- may be hypotonia, hypoglycemia.
- Short stature.
- Rounded head.
- Prominent head.
- Broad face.
- Depressed nasal bridge.
- Saddle small nose.
- Undeveloped Mandible & chin.
- Short neck.
- Proportionate limbs with small hand & feet.
- Underdeveloped genitalia & absent body hair.
- Normal IQ.
- Initially normal, then growth failure.
- Multiple hormonal : - TSH – ACTH – ADH – GnTH - GH
- Headache, vomiting, squint.
- Recombinat human growth hormone (r HGH). S.C
- Replacement therapy for other hormones.
a- Hypogonadotropic conditions | b- Hypergondotropic conditions |
1- Multiple pituitary horm. . 2- Isolated G.H. . 3- Isolated GnTH 4- Syndromes (Parder - Willi syndr). 5- Systemic dise.: Nutritional, psychologic. 6- Other endocrinal cause: hypothyroidism. Hyperprolactinemia. 7- Polycystic ovary dise. 8- Constitutional delay in growth. | 1- Ovarian and testicular dysgenesis. 2- Enzyme defect. 3- Androgen in sensitivity. 4- Gonadal toxins or radiation ttt. 5- Other miscellaneous causes. |
Central:
Idiopathic true precoious pouberty.
CNS disorders ( meningitis, encephalitis ) .
CNS tumors ( Hamartoma, hypothalam. Tumor ).
Peripheral:
Male
A- Adrenal tumors
C- Congenital adrenal hyperplasia.
L- Leyding cell testicular tumor.
T- Testotoxicosis.
Female
- Adrenal tumors.
- Ovarian tumors
- Follicular cysts.
- Exogenous estrogen.
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